Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.
- NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_assertion description "[We conclude that the 5q-syndrome may be best defined as primary MDS of the FAB type RA with a 5q deletion as the sole karyotypic abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.
- NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_assertion evidence source_evidence_literature NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.
- NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_assertion SIO_000772 7604812 NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.
- NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_assertion wasDerivedFrom befree-20150227 NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.
- NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_assertion wasGeneratedBy ECO_0000203 NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP873053.RAdCwNQ5TnrypltuJWaL422Z1AQckI9cuzU0p0pVAi6PY130_provenance.